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  • Lass, Amir  (4)
  • 1
    In: Pharmacoepidemiology and Drug Safety, Wiley, Vol. 32, No. 1 ( 2023-01), p. 78-83
    Kurzfassung: As part of the European risk management plan of a 91‐day extended levonorgestrel‐containing combined oral contraceptive (COC LNG ), a study was performed to assess its safety. This analysis was conducted to examine delayed pregnancy detection and return to fertility with extended combined oral contraceptives (COC). Methods We conducted a retrospective cohort study in new users of 91‐day COC LNG or 28‐day COC LNG within a US‐based healthcare claims database from 2006 to 2017. Delayed pregnancy detection during current COC LNG exposure was defined as the time between estimated pregnancy start and first prenatal care encounter. Additionally, the time between estimated pregnancy start and COC LNG discontinuation was measured. To measure return to fertility, pregnancy rates were estimated among females who discontinued treatment. 91‐day COC LNG users were propensity score‐matched to 28‐day COC LNG users. Hazard ratio for pregnancy was calculated using Cox proportional hazards models. Results The 91‐day and 28‐day COC LNG users had 25 593 and 76 586 treatment episodes, respectively. The median time to pregnancy detection was 64.5 and 61.0 days ( p  = 0.24) in users of 91‐day COC LNG and 28‐day COC LNG . The median exposure time to treatment after estimated pregnancy start was 54.0 and 38.0 days ( p   〈  0.01). In the fertility analysis, pregnancy rates were 54.82 (95% CI, 50.05–59.93) and 69.30 (95% CI, 64.98–73.82) per 1000 person‐years in extended COC LNG discontinuers and 28‐day COC LNG discontinuers. The adjusted hazard ratio of pregnancy was 0.77 (95% CI, 0.69–0.85). Conclusions Small differences were observed for pregnancy rates and delayed pregnancy detection between 91‐day extended COC LNG and 28‐day COC LNG , which may be related to the longer days' supply of extended COC LNG . Differences in the fertility analysis may be related to unmeasured residual confounding.
    Materialart: Online-Ressource
    ISSN: 1053-8569 , 1099-1557
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2023
    ZDB Id: 1491218-1
    SSG: 15,3
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    In: Contraception, Elsevier BV, Vol. 105 ( 2022-01), p. 26-32
    Materialart: Online-Ressource
    ISSN: 0010-7824
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2022
    ZDB Id: 2004856-7
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    Frontiers Media SA ; 2021
    In:  Frontiers in Endocrinology Vol. 12 ( 2021-3-16)
    In: Frontiers in Endocrinology, Frontiers Media SA, Vol. 12 ( 2021-3-16)
    Kurzfassung: Ovaleap ® (follitropin alfa), a recombinant human follicle stimulating hormone, is a biosimilar medicinal product to Gonal-f ® and is used for ovarian stimulation. The main objective of this study was to assess the safety and effectiveness of Ovaleap ® compared to Gonal-f ® in one treatment cycle in routine clinical practice. Methods Safety of Ovaleap ® Follitropin alfa in Infertile women undergoing superovulation for Assisted reproductive technologies (SOFIA) was a prospective cohort study conducted in six European countries. Eligible patients were infertile women undergoing superovulation for assisted reproductive technology, who were administered Ovaleap ® or Gonal-f ® for ovarian stimulation and were naïve to follicle stimulating hormone treatment. The recruitment ratio was 1:1. The primary endpoint was incidence proportion of ovarian hyperstimulation syndrome (OHSS) and the secondary endpoint was OHSS severity (Grades I, II, III). The effect of risk factors or potential confounders on the odds ratio for OHSS incidence as well as treatment effect on OHSS incidence was explored using univariate logistic regression. Pregnancy and live birth rates were also assessed. Results A total of 408 women who were administered Ovaleap ® and 409 women who were administered Gonal-f ® were eligible for analysis. The incidence proportion of OHSS was 5.1% (95% CI: 3.4, 7.7) in the Ovaleap ® cohort and 3.2% (95% CI: 1.9, 5.4) in the Gonal-f ® cohort. This difference in OHSS incidence proportion between the two cohorts was not statistically significant neither before (p = 0.159) nor after univariate adjustment for each potential confounder (p & gt; 0.05). The incidence proportion of OHSS severity grades was similar in the two treatment groups (3.4% versus 2.0% for Grade I, 1.2% versus 1.0% for Grade II, and 0.5% versus 0.2% for Grade III, in the Ovaleap ® and Gonal-f ® cohorts, respectively), without a significant statistical difference (p = 0.865, for each grade). Among patients who had embryo transfer, clinical pregnancy rates were 33% and 31% and live birth rates were 27% and 26%, in the two cohorts, respectively. Conclusions Findings from the SOFIA study indicate that the incidence proportions of OHSS and OHSS severity, as well as pregnancy and live birth rates, are similar between Ovaleap ® and Gonal-f ® treatments and corroborate the safety and effectiveness of Ovaleap ® as a biosimilar to Gonal-f ® .
    Materialart: Online-Ressource
    ISSN: 1664-2392
    Sprache: Unbekannt
    Verlag: Frontiers Media SA
    Publikationsdatum: 2021
    ZDB Id: 2592084-4
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    Informa UK Limited ; 2021
    In:  Current Medical Research and Opinion Vol. 37, No. 3 ( 2021-03-04), p. 515-522
    In: Current Medical Research and Opinion, Informa UK Limited, Vol. 37, No. 3 ( 2021-03-04), p. 515-522
    Materialart: Online-Ressource
    ISSN: 0300-7995 , 1473-4877
    Sprache: Englisch
    Verlag: Informa UK Limited
    Publikationsdatum: 2021
    ZDB Id: 2034331-0
    Standort Signatur Einschränkungen Verfügbarkeit
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